Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.30304580dup , CM000685.2:g.30304580dup | GRCh38 |
| NC_000023.10:g.30322697dup , CM000685.1:g.30322697dup | GRCh37 |
| NC_000023.9:g.30232618dup | NCBI36 |
| NG_009814.1:g.9801dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000378970.5:c.*1dup MANE Select | ENSP00000368253.4:n.*1dup | |
| ENST00000378970.4:c.*1dup | ENSP00000368253.4:n.*1dup | |
| NM_000475.4:c.*1dup | NP_000466.2:n.*1dup | |
| NM_000475.5:c.*1dup MANE Select | NP_000466.2:n.*1dup |